GT PK Comparison, Dose Scaling, And Promoter Section
GT PK comparison (continuation)
| Affected by | Capsid | Distribution → cell uptake (ie transduction) → intracellular trafficking → degradation of vector in the cell - Secretion (so shedding marker) - Can be affected by immune responses - Durability of VS (ie loss of episomal DNA) | Transcription rate from DNA to mRNA (특히 이부분이 종간차 커서, NHP은 mouse 대비 수십배까지 적음, 더구나 human potentially has 3x lower transduction & expression efficiency than NHP)(1 vg당 1 mRNA copy니 오시 않고 보통 수십개 나옴. - mRNA stability - secretion (글 수 있음) | - Translation rate from mRNA to protein (낭연히 1 vg낭 1 protein 나오는 것이 아님! - Secretion (글 수 있음) - Can be affected by immune responses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 20210210 Translational science forum | Capsid concentration assay may build an exception as established AAVx ELISA may not be feasible for novel (engineered) capsid. | 이건 PK 에 불포함 | - | - | 이것도 pk에 포함 (TG product 임) | 이것도 pk 에 포함 (TG product 임) | - | - | - | - | ||
| Hunter,, TAK-073 | 여러 dose 의 rAAV-GT vg/kg (Mouse) 두 dose 의 rAAV-GT vg/kg (NHP) | 안 보네? 안 보네? | I2S (Serum & tissue) I2S (Serum ) | Not shown, (correlate) I2S activity | - Not shown | ↓ GAG - | ↓ LAMP1 (IHC, for lyso vol) Normal NHP 라 무의미 | - - | ||||
| Fabry | rAAV-GT vg/kg (Mice) rAAV-GT vg/kg (Human) | αGal (serum & tissue) αGal (serum & tissues) | Gb3 & Lyso-Gb3 (tissue) Gb3 & Lyso-Gb3 (tissue) | |||||||||
| hemophilia | rAAV-GT cp/kg (Human) cp is capsid particle | FVIII | FVIII activity | |||||||||
| DMPK: no need to measure (Parkin GT meeting) | The correlation between vector and DNA may not be linear (eg. DNA production may be saturated) Parra-Guillén2010 | |||||||||||
| assay | AAVx ELISA may not be feasible for novel (engineered) capsid. | qPCR | RT-PCR | ELISA | ||||||||
| Discriminate transgene? | NA |
- shire ID tag qPCR (GBA GT preclinical) - GBA GT (Pharm Sci): the ID-Tag (target region for the dose measurement assay) is incorporated into all potential transgene candidates - Frataxin gt: NHP biodistribution studies for StrideBio's lead capsids will be performed with a HA-tagged version of the lead expression construct. • For the lead cassette epitope tagged versions are being developed which are necessary for biodistribution studies in NHP. Human influenza (HA) tag in 3 different versions and Myc-tag are considered. |
- Sarah Melissa Jacobo: anti-human Parkin (or anti-HA antibody) 가 혹시 있으면 endogenous parkin과 구분할 수 있을지도 (mouse와 구분에 국한될 듯) - While the antibodies against frataxin protein can discriminate between mouse and human, they do not discriminate between NHP and human (어쨌든 Clinical study에서는 무상관) | - | - | - | - | - | - | |||
|
- 구분 필요 없을 듯: Because 이차피 Transgene-specific PD 안 존재 - 구분 필요 할 듯, because • Endogenous protein 의 functional viability 모르므로 (반론: gba환자에서 대개 gba amount 와 activity가 비례함) | - | - | - | - | - | - | ||||||
The average life span of adult human hepatocytes is around 500 days (20210207 Estimation of Human Efficacious Dose TSF GT modeling)
Dose Scaling for GT
DoseHuman = DoseAnimal · (Scaling factor) · (Activity factor)
- DoseAnimal
- Pharmacologically active dose (PAD; usually in vg or vg/kg) in animal models
- No-observed-adverse-effect level (NOAEL) dose in toxicological species
- (Scaling factor)
- Scaling factor based on:
- Body weight, or
- Target organ volume
- Scaling factor based on:
- (Activity factor)
- “Relative activity factor” based on perceived species difference in transduction
- Examples:
- Internal hemophilia GT programs cited a mouse-to-human factor of 30
- Mouse-to-human factor of 20 to 100 from external programs
- NHP-to-human factor: Key issue #1
Species difference (Activity factor)
아래 표 의미: mouse 에서 NHP 거쳐 human 으로 가면서, vg (biodistribution)도 줄고, mRNA 도 줄고, protein 생산도 줄어, 종국에는 human 이 120 배 준다. (from 20221005 Tomoki_modeling strategy for NS GTs for PRKN GT.ppt)
| Analytes | Mouse | NHPs | humans |
|---|---|---|---|
| Vg | 0.7-3.8x | - | |
| mRNA | 57-134x | - | |
| Transgene proteins | - | 2.9x | |
| Overall | ~120x (previous benchmark) | ||
참고: gene efficiency factor (GEF) ({Tang, 2021 #2153})
Scenarios of Objectives of dose exploration in P1 (
- MTD
- Range of optimal effective doses
- achieving a specified target range of exposure that was derived by significant practical limits on the dose of the product that can be produced or delivered
stopping rule, treatment plan (staggering administration ) 등 관해 fda guidance (Considerations for the Design of Early-Phase Clinical Trials of Cellular and Gene Therapy Products) 봐라!
Promoter
| (P)1 | Relatively small size (1,179 bp), which is good |
enhancer 와 promoter 와 intron 는 붙어다니는구나.
- (CAG?)I: CMV early enhancer fused to modified chicken β-actin promoter
- (CAG?)G: CMV early enhancer fused to modified chicken β-actin promoter
- V: Human cytomegalovirus immediate early enhancer/promoter
- K: phosphoglycerate kinase 1 promoter
- C: Human ubiquitin C promoter
- A: Human eukaryotic translation elongation factor 1 α1 promoter
(EF1A short form): Human eukaryotic translation elongation factor 1 α1 short form
Table 1
Comparison of Selected Ubiquitous and Cell-specific Promoters.
| Promoter | Specificity | Relative Strength | Size (bps) | Reference(s) |
|---|---|---|---|---|
| CMV | Ubiquitous | +++ | 750–800 | Xu et al., 2001; Gray et al., 2011 |
| CBA (including derivatives: CAG, CBh, etc.) | Ubiquitous | +++ | 248–1,600 | Klein et al., 2002; Ohlfest et al., 2005; Gray et al., 2011 |
| EF-1α | Ubiquitous | ++ | 2,500 | Gill et al., 2001; Xu et al., 2001; Ikeda et al., |
| UBC | Ubiquitous | + | 403 | Gill et al., 2001; Qin et al., 2010 |
| GUSB (hGBp) | Ubiquitous | + | 378 | Husain et al., 2009 |
Uncertain Spans
| location | transcription | uncertainty |
|---|---|---|
| GT PK comparison header (NHP transduction note) | (1 vg당 1 mRNA copy니 오시 않고 보통 수십개 나옴. | The Korean note is partly wrapped onto a thin column; tokens 오시 않고 may be a transcription of 오지 않고 (“does not come”), but the visible glyphs remain as written. |
| GT PK Hunter,, TAK-073 row | 안 보네? (twice) | The same text fills two adjacent merged columns; the source likely intends one statement spanning both columns rather than a duplicate, but the rendering here preserves both visible cells. |
| GT PK assay row | qPCR / RT-PCR / ELISA row alignment | Three sparse cells are spread across many narrow columns in the source; column-cell alignment beyond the visible labels is not fully reconstructed. |
| Promoter abbreviation list | (CAG?)I and (CAG?)G | Two leftmost abbreviations are partly obscured by the Promoter heading and a leading paren glyph; both appear to point to CAG-style enhancer/promoter combinations but the exact key letter is not legible. |